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Special Report                                                                   Special Report


 synthesized by controlling the Pd load-  High-effi ciency direct   sured  activity and  chemical composi-  catalyst partially dissolves under hydro-
 ing  amount  and preparation  methods,   esterifi cation of CO  and   tion is reported. (Ind. Eng. Chem. Res.,  formylation  conditions.  Cyclohexene
                           2
 on the title  conversion of practical   methanol over Co-doped CeO    2025; DOI: 10.1021/acs.iecr.5c00026).  was  used  as  an  olefi n  at  40  bar  and
 interest. The nanocluster catalyst gave   catalysts  2                   100°C.  Heterogeneous separation was
 relatively  high hydrogenation  activity.   Enhanced stability and       done. Long-chain C -C alkenes, alpha-
                                                                                             18
                                                                                          6
 (Chem. Commun., 2025/DOI:10.1039/  C. Xue et al have worked on the title   activity in upgrading ethanol   methylstyrene and mixed octenes were
 cent breakthrough and perspectives are  monomers  in  up  to  98%.  Blends  of  D4CC05105J).  reaction to make dimethyl carbonate   (E) to n-butanol (B) using a   studied. (Ind. Eng. Chem. Res., 2025;
 discussed. (ChemSusChem, 2024; DOI:  polymers can also be processed.  (DMC; which is obtained via exchange   Ru polyphenylene catalyst  DOI: 10.1021/acs.iecr.4c03886).
 10.1002/cssc.202402335).  Ketonization of valeric acid to   reaction of  ethylene carbonate with
 Inverting methanol   5-nonanone  CH OH). The chemical stability of CO    X.  Pei  et  al have  compared homo- Production of xylenes from
         3
                                      2
 Catalyst improved   dehydrogenation selectivity   makes this reaction diffi cult. A series of   geneous and heterogeneous catalysts in  heavy reformate (HR)
 stereoselectivity and   by crowding atomic Ni species   A.A. Eslami et al have screened metal   catalysts M-CeO  (M= Fe, Cu, Co, La,   Guerbet chemistry. There is a reference
                    2
 regioselectivity control to   over α-MoC catalysts  oxides  for  the  title  reaction.  Good   Zr, Ni, and Al) were constructed by a   to catalyst compatible  with molecular   HR contains pseudocumene, ethyl tolue-
 access completely alternating   catalysts have both lattice  energy and   sieves for water removal, which results   nes, mesitylene, etc. and T. Kella et al
 poly(lactic acid-co-glycolic   Y. Ge et al have referred to metal car-  amphoteric properties. ZrO  was found   in enhanced B yields. In situ reduction   have worked on converting this C9+
 2
                                                                          cut into xylenes. This review highlights
 acid) (PLGA) with enhanced   bides as promising alternatives of noble  to be the most active catalyst. Tempera-  of Ru polyphenylene catalyst was car-  the role of zeolite catalysts in improv-
 properties  metal  catalysts. However, the precise  ture was in the range of 350-450°C.   ried out to form Ru nanocluster during   ing product selectivity and focuses on
                                         Guerbet reaction. Detailed functioning
 control  of reaction  pathways  on them  The catalysts were fully characterised
 remains a formidable challenge. When  and by products were also analysed.   of the catalyst  is reported.  (Applied   catalyst  modifi cations  and  topologies.
 X. Guo  et al have referred to the   α-MoC  is  decorated  with  crowding  (ChemCatChem., 2024; DOI: 1002/  Catalysis A:  General, 2025, 694, 25   The effects of  incorporating various
 title  polymer as an ideal candidate   atomic Ni species, CH OH goes to CO  cctc.202401467).  March, 120139; DOI:10.1016/j.apca-  metals in zeolites on the product selec-
 for controlled  drug delivery.  These   + H .  Under  optimal  conditions,  ex-  doping strategy. 2-Cyanopyridine (CP)  ta.2025.120139).  tivity and yield are reported. Aspects of
 3
 2
 authors have used the chiral (BisSalen)  cellent selectivities of the target com-  Molecularly defi ned lubricant   was employed  as a  dehydrating  agent   catalyst deactivation and  regeneration
 Al catalyst,  which promoted a robust   pound (over 90%) can be achieved in   hydrocarbons from olefi n   to  facilitate  the  esterifi cation  reaction.   Glycerol (G) to AA  are discussed. Aspects of reactor engi-
 polymerisation of enantiopure 3-methyl   both cases  with unprecedented pro-  Under  optimal  conditions  61%  con-  neering and process optimisation  are
 glycolide with  highly glycolic site   duction rates  of  methyl formate and   metathesis  version of CH OH with 61.6% yield of  A. Kurniawan  et al have investigated  also covered. (Ind. Eng. Chem. Res.,
                  3
 selectivity,  giving  alternating  PLGA   H  for different versions of the catalyst.  Z.J.  Berkson  et  al  have  referred  to   DMC was realised. Monomethyl  car-  the gas phase conversion of G to AA  2025; DOI: 10.1021/acs.iecr.4c03940).
 with regioselectivity. Degradation and   Kinetic, spectroscopic and computa-  the use of hydrocarbons based syn-  bonate was an intermediate. (Ind. Eng.  through consecutive dehydration and
 2
 drug  release  experiments  were  done.   tional assessments  were integrated to  thetic  lubricants.  Branched  terminal   Chem. Res., 2025; DOI: 10.1021/acs.  H  transfer reactions over Mo-V oxides  Transalkylation between
                                          2
 (Angew. Chem. Intl.  Ed., 2024; DOI:   clarify the mechanism of the above re-  olefi ns were used and after metathesis   iecr.4c04628).  supported  on  acid-modifi ed  montmo- C  aromatics and
                                                                            10
 10.1002/anie.202417075).  markable selectivity inversion. (Angew.  were subjected  to hydrogenation. An-  rillonite (HMMT). The use of HMMT  2-methylnaphthalene
 Solvent-free chemical   Chem. Intl. Ed., 2024; DOI:  10.1002/  alytical  procedures were employed   In situ reduced Ni-Sn   as a support enables the well dispersion  (MN) to synthesize
                                         of  metal  oxide  particles  with  nominal
 recycling of polyesters and   anie.202023682).  to characterize the products. (Chem-  bimetallic catalyst for   loadings up to 5 wt % on the catalyst   2,6-dimethylnaphthalene
 polycarbonates by Mg-based   CatChem., 2024; DOI:  10.1002/cctc.  enhancing direct upgrading   surface while the acidic sites facilitate   (DMN) by Mo-modifi ed
 Lewis acid catalyst  From single atoms to   202401590).  of aqueous ethanol to higher   dehydration of G to acrolein with 74%   HZSM-12 catalysts
 nanoparticles: Size effect on
       alcohols
 W. Zhao et al have utilised commercially  Pd/C-catalysed hydrogenation   Carbonylation reactions using   selectivity. At 320°C and ambient pres-  DMN is a key raw material  to make
 available Lewis acids (LAs) to realize  of 2,5-furandicarboxylic acid  single-atom catalysts  B. Chen et al have investigated NiSnH  sure, 22% yield of AA is reported. (Ind.   the  corresponding  dicarboxylic  acid,
 closed-loop recycling through the cata-  L. Jurado  et al  have reviewed the re-  catalysts under various gas atmospheres  Eng. Chem. Res., 2025; DOI: 10.1021/  which in turn is used to make polyethy-
 lytic  depolymerisation  of aliphatic  J. Zheng  et  al have reported  a study   cent advances in tailoring solid sup-  and pretreatment temperatures and this  acs.iecr.4c02838).  lene  naphthalate  (PEN),  which  has
 polyesters and polycarbonates.  Thus  of fi ve catalysts with Pd particle sizes   ports for single-atom catalysts (SACs)   have infl uence on the title conversions.   some outstanding properties compared
       Theoretical  insights  are reported and  A carrier-free recyclable
 poly(ε-caprolactone)  and  poly(trimethy-  ranging from single atoms to nano-  to enhance their catalytic performance   to  PET.  C.  Xiong  et  al have  made  a
 lene carbonate)  were  converted to  clusters and nanoparticles, which were   correlative  dependence between mea-  Rh/Terpyridine catalyst for   series of Mo/HZSM-12 molecular sieve
 in the title reaction, hydroformylation,   alkene hydroformylation:      catalysts for the title reaction. The trans-
 methanol carbonylation, and oxidative   Homogeneous catalysis and        alkylation reaction was done under H
                                                                                                         2
 carbonylation. Optimizing of solid sup-  heterogeneous separation        atmosphere.  30% Mo/HZSM-12 gave
 ports to realise highly active and selec-                                excellent  performance  with  61%  con-
 tive performance is discussed. In situ/  H. Fang et al have synthesized a new  version  of MN and 2,6- to 2,7-DMN
 operando characterisation  of the cata-  square-planar geometry Rh (I) com-  ratio of 1.69. (Applied Catalysis, 2025,
 lyst is covered. (ChemCatChem., 2024;   plex,  Rh (CO) (Terpyridine)  and pro-  693, 5 March, 120138; DOI:10.1016/j.
                                                1
 DOI: 10.1002/cctc.202400543).           perly characterised the catalyst.  This  apcata.2025.120138).

 180  Chemical Weekly  April 8, 2025  Chemical Weekly  April 8, 2025                                   181


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